lx7101

LX7101是 LIMK 和ROCK2高效抑制剂，对LIMK1 2、ROCK、PKA 的IC50分别为24、1.6、10 和小于1 nM。

LX7101 is a potent inhibitor of both LIM kinase (LIMK) 1 and 2, and Rho-associated kinase 1 (ROCK1) and ROCK2, with IC50 values of 32, 4.3, 69, and 32 nM, respectively. It is selective, demonstrated by its lack of cross-reactivity in a panel of binding assays involving 78 receptors, transporters, and an additional 430 kinases, at a concentration of 10 μM. The topical administration of LX7101 (3 μl of a 1 mg ml solution) to the eye has been shown to reduce intraocular pressure in a dexamethasone-induced mouse model of glaucoma.

LX-7101 hydrochloride是高效的 LIMK 和 ROCK2 抑制剂，具有降压活性，抑制 LIMK1 2, ROCK, PKA，可用于研究青光眼。